Fish oils symptoms and conditions

I am 50, pretty healthy, but have had a new condition of inflamed and severely painful joints and muscles limiting activity. Doc put me on 60 mg prednisone for 3 days, then 40 mg 3 days and 20 mg 3 days. First day was ok. Since then I have been a raving lunatic! I read the post about the person chasing their cat around and had to laugh and relate. I flipped off the neighbors workers because they were backing up a truck and it was noisy! It is all I can do to keep myself in check. I have canceled/rescheduled all unnecessary appointments until next week when I am finished. I "sleep" about 3 hours a night. Last night I peed the bed. I eat constantly. I have to work and concentrate (teach college) and that is so hard. I imagine my students must think I am on meth. I can't take it any more. I have 1 day left and I am not going to take the last one. I hope that this regimen will have calmed down the inflammation and if it recurs I will seek alternatives. AM NEVER going back to prednisone unless it is life or death situation.
Good luck to all those out there who have to take it long-term. Bless your hearts.

I was taking Lamictal for 2 years. I was diagnosed with a "light" case of bi-polar. Not the highs, only the lows. I am not too sure that I wasn't just going through some really rough times in my life and had had enough. Couldn't take the stress. Anyway at first I had dry mouth, bad constipation, belching in the evenings and lots of it, some female itching and similar issues (sorry but just want to help here), couldn't handle any alcohol, loss of hair, problems sleeping, outbursts of anger towards mate and irritability, aggressiveness at time, loss of memory and loss of concentration, scatteredness, lots of hair loss and sensitivity to sun. I wanted to be a trooper and make my psychiatrist happy so stayed on it. I got lots of good things from it, like can roll with the punches of life better, can really easily speak up for myself and defend myself when I need to. Don't beat myself up like I used to. So, lost some of the sensitivity that I needed to lose but can't do without my memory. It had been so bad that friends and family would comment and I was embarrassed. Also, my mate shouldn't have had to deal with some of the rage that would show up when things were taken wrong. Oh, I had one of the strongest panic attacks that I can imagine a person living through. I had never had one before, and haven't had one since. I stopped this drug cold turkey. It felt like a few weeks of jet lag. Take multi-vitamins and minerals, also fish oils. Only the highest quality. Eat really healthy, exercise, drink lots of water and rest a lot...whatever you do, don't stress out if you are coming off of this drug. This is actually a very useful medication, however, in my opinion it needs to have more research done about it.

My mother, 70 years old, been on Coumadin for 3 years (doctor said best to take since she suspected heart palpitations). Mother developed gradual memory loss, over the 3 year period, we didn't think anything wrong!! just a part of aging process!! Then one night she fell on the floor, stroke, we took her to hospital - done MRI and CTscan - result: severe brain bleeding. From that time - 4 months ago - she is now diagnosed with Dementia. I cant even describe how I feel about god damn Coumadin. Wish they never given it to her in the first place.

Some good news re: my concerns in my Drs. note (posted the other day) "some buildup" and why such a high dose 40mg. of this poison?. I actually received something from the cardiologist on Fri. which made me feel much happier. 'NO SIGNIFICANT ABNORMALITIES - MILD CHOL. PLACQUE BUT NO SIGNIFICANT BLOCKAGE SEEN' so you can imagine how much better I felt - I had already made the decision to not take the Statins, but that report absolutely convinced me. If you haven't already had a doppler on your carotids, do so, it can ease your mind, since we're always being told we're clogging up our arteries with just about anything and everything, we're gonna have a stroke, etc. all these scare tactics. It's not an expensive test (about $80, not sure what will be added to that, as to cardio. reading the results), but worth it. Read up on the Red Yeast Rice - I've read several articles from several well known medical websites - it seems it actually can work better than Statins! Get off this stuff people, more risk than having a stroke!

I am currently 58 years old and lead a very active, healthy lifestyle. I began taking 10mg of Zocor, along with 1000mg of niacin in the summer of 2004 to reduce cholesterol (251) and triglycerides (571). The therapy dramatically improved my blood tests, however, within 6 weeks, I began to experience minor chronic skin infections, both fungal and bacterial. They were easily controlled with topical over the counter type medications, but they were annoying. At no time was this new condition linked to the statin/niacin therapy by my doctor(s). The infections became progressively worse over the next 3 years, and evolved into chronic folliculitis in my scalp, neck, and face, cystic acne, and persistent fungal infections that were becoming more difficult to control. In addition, I began to get chronic eye infections. It was as if my immune system was becoming ineffective. I stopped taking niacin in December of 2007 and the symptoms immediately lessened. I stopped taking Zocor in March of 2008 and within 2 weeks, all the skin problems and eye infections completely ended. My health was restored completely and I am glad to have put that whole mess behind me! I have been taking Omega 3 supplements to control my cholesterol and triglycerides and have had results that equaled the Zocor and Niacin therapy, with cholesterol at 160, triglycerides at 91, and a favorable HDL/LDL ratio. My physician is skeptical, but I know that my body was not functioning correctly with the statin/niacin treatment. I have found anecdotal reports from others who seem to have experienced a change in their immune system, but no mention of this as a side effect by the medical establishment.

I was taking Lovastatin until the VA told me that it was not on their formulary any longer and I had to take Simvastatin. Within a couple months my feet started burning and a numbness began creeping up my legs. I began falling, staggering and lost the ability to walk without two canes. I thought I was in the early stages of MS or ALS and feared I was dying. My fiance' did research on the internet (Spacedoc.com) and discovered that the symptoms I was suffering from were the result of Statin Poisoning (don't take my word...look it up) I took myself off the Simvastatin at the doctors request and began taking 4 1000mg of Omega 3 Fish Oil, 2 50mg CoQ10, 1 50mg L Carnitine, a multi vitamin, and 1 81mg coated aspirin per day. I still have numbness in my legs and some burning in my feet one and one half years later. My Neurologist has told me (and written a letter to the effect) that I am permanently disabled...that this will never go away. Statins (all Statins) are poison...don't take them....the pharmacutical companies only push them to make MONEY they don't care about you or your health. If you need more information contact me anytime and I'll be happy to share any research I have. ******

I am 53 years old and was almost 4 years on Lipitor and started experiencing periphial neuropathology that was horrible! I had a keen neurologist who took me off after doing several tests for Lyme, Lupus, MS, etc. She said she sees more and more of my symptoms 3 to 8 years plus on Lipitor. I went off Lipitor on June 1st (my birthday), so have been off for more than a month. All of the zapping and tingling has subsided in my hands, feet, face, arms, and head. I still have neuropathology in my hands, some muscle weakness in my arms, and numbness in my toes which are all slowly diminishing. My neurologist says she expects full recovery in 4-6 months. Take B complex vitamins. I take Shaklee's twice a day.This greatly helps in the repair of the nerve damage from Lipitor. My neurologist also recommended me taking FBCx, ******(1-2 with every meal containing fat, the website explains dosage), and 1 tablespoon of omega 3 fish oils in the form of flax or fish to reduce cholesterol. There are other things I take like garlic, cinnamon extract, green tea extract. If you type in "lower cholesterol with supplements" online you will find other things like red rice yeast as well. Good luck!

My father is currently in the hospital for his second internal bleeding from coumadin. He had a GI bleed and was discharged a month ago, put on coumadin AGAIN , supposedly monitored and wound up in ICU again, this time he had trouble breathing and was intubated and sedated for two days. I really thought Coumadin killed my father and in reality it almost did.....Now the hematologists are saying he is extremely sensitive to it, and his only other option is heperin shots which he refuses to do (that also has risk of bleeding). he is going to live with the chance of stroke rather than take coumadin a thrid time which is what they are suggesting. (idiots) . he has atrial fib and needs to be on blood thinner but at this point he would rather take his chances or take aspirin even though the doctors are saying it won't work as well. Hopefully there will be new anticoagulants out in the market soon like there are in Canada and Europe.

Coumadin KILLS....8,000 people a year bleed to death from coumadin......yes, it helps people too but judging from this site the side effects are awful...if you can avoid coumadin you should...

Hello,
I am following up with my father's case that I wrote about in January,(jb4boys). He is 77 and I took him off of Lipitor on my own on Feb. 4,2008. We have yet to tell his primary physician, but have told the arthritis specialist I took him to 3 weeks ago. The tingling going up his arms has stopped and he is sleeping better, hands still hurt, but are getting better. I have started him on fish oils- omega 3. Am told that the Omega 3 DHA and EPA totals need to be over 1000, and actual fish (sardine, anchovy, etc.). Bloodwork from arthritis doctor showed no arthritis, but x-rays did show swelling in hands and feet. He was on Lipitor for 7 years, so it will take a while for him to get rid of this drug in his system. Have heard that Lipitor attacks the muscles, joints and then the heart. I can honestly say that I have not heard of 1 person with a positive comment about this drug. Find another way to control your cholesterol, there are many natural supplements that have been proven to help - with no side effects. Have also heard that wellness doctors and acupuncture is another natural way to lower your diabetes, cholesterol, hbp - all natural.
Good luck and keep in touch with how you are progressing.

Hello, I will appreciate if someone help me get rid of my MOON FACE and the pain in all my joints

I just started 80 mg of Prednisone for Vasculitis in my kidney’s. I also have RA. This treatment is being augmented with low dose chemotherapy. The Chemo is nothing compared with the side effects of the Prednisone. It is Horrible. It has so messed with my brain I never knew what an awful existence obsessive compulsives live. I can’t sit still and stop doing things if there is anything left undone! I have trouble with controlling my emotions, responses etc. Thinking isn’t easy either. And I’m awake most of the night. (Not a bad thing since we just were blessed with twins however). But it is really straining my relationship with my 6 year old son who can’t understand why his Dad goes from nice dad to mad dad in a second. I’ve also have horrid muscle fatigue in my legs. For me this is the worst because getting up and moving and walking up stairs is almost impossible. And I was hiking up to 5 miles in rough terrain just a few weeks ago. I’ve actually LOST 10 lbs.

So I am wondering if anyone has any tips, tricks or ideas they have found to combat the muscle fatigue? It would be greatly appreciated if you could share any ideas you have. I’ve been drinking water and electrolyte replacements, (G-2, the new Gatorade) but that has not solved the problem.

Thanks.

I was just wondering...I've been weened off Prednisone the last month or so and today is my last pill. YEAH!!!!!!!!!!!!!!!!! AMEN!!!!!!!!!!!!!!!!!!!!!.
However, I've noticed that my joints hurt and my feet oh the pain. Is this normal. I feel like my muscles are weak. walking up a flight of stairs is painful. Anyone know how long this will last or if this is something I will have to live with.

I am 21 years old and was recently diagnosed with rheumatoid arthritis in my hands, fingers, and wrists. My doctor put my on 60 mg of prednisone at first and then had me slowly go down to 20 mg a day. I have since been trying to go off of it myself. I can't stand the side effects any longer. I have this constant charlie horse pain in my hips and legs, i am so hot and constantly flushed, i feel so depressed ( i am normally a happy all smiles kind of person ) i have done nothing but cry everyday for the past week because I just feel like so many people don't understand or believe anything I am saying. I thought maybe some of this was all in my head until I found this site. Is there any other medications out there that don't have all these terrible side effects? I feel as though the pain from the arthritis is far less worse than this.

PLEASE REPLY! ok i wrote on this board about a month ago, and i was complaining about all the horrible side effects i was having.....however things have gotten much much worse since then, and i must admit that i have been bad. very bad. i am secretly winging myself off of the steroids b/c I cannot handle the depression and not being myself anymore... I've been on Prednisone for a year now and started winging myself from 15mg when I last wrote on here to now 10 mg... my hair is falling out in HUGE clumps, and I am NOT overexaggerating when I say I am going bald... does anyone know if this could be from tapering the drug, or would you say it is probably because of my condition possibly returning from tapering the drug too low???? I just want to know if IMMENSE hair loss is affiliated with steroids...I have not seen anyone else mention anything.

I must add my recent experience with Prednisone to this forum:

I have been suffering from constant lower back pain and a torn shoulder injury (rotator cuff) for the last several years. A week ago I got a slight case of Poison Ivy. My doctor gave me Prednisone - starting at 60 mgs. a day, tapering down to 10 over 12 days. I was unsure as to whether I wanted to be on a steroid , especially after reading some of the testimonies here at this forum. But I went ahead and took it. I must say this has been one of the most amazing experiences for me.
Not only did my Poison Ivy immediately begin to go away, but lo and behold, practically ALL my back pain and shoulder pain went away. I also found myself with this amazing positive mental attitude. I began to get up and enjoy my job everyday (normally I am somewhat depressed and stressed out). It was such a major change for the better - I feel like I have been living the resurrection!! Yet I know it is only due to absence of pain and increased energy brought on by the Prednisone. I feel like a happier, younger version of myself. Prednisone has even helped me sleep better! So, evidently, for some people, prednisone is a wonder-drug.
I did note a very slight manic edge at times, but never unmanageable and always very positive. As soon as I decrease the dose, the pain and inflammation in my back and shoulder starts to return. What a shame that this drug causes osteoporosis and other long-term affects. I wish I could stay on it forever!!

My Mother was diagnosed with Rheumatoid arthritis 30 years ago. She has been on prednisone at low doses since then. About 3 years ago she started imagining things, and hallusinations. About 2 years ago her prednisone dose went up to 60mg a day due to a stroke of the optic eye nerve. She has since been tapering down, now at 15mg a day. But tapering down makes her arthritis more painful. She has developed diabetes, loss of sleep, loss of apetite, loss of muscle tone. When she gets bumped, it's a big opened gash, rather than just a bruise. With the higher dose she was more moody & would get angry easier. The hallucinations & paranoia continue & are making me more & more concerned. I haven't read about this in any of the stories. Has anyone else experienced this side effect? I spoke with her Rheumatologist who suggest a psychiatrist to prescribe anti-psychotic drugs. She's already on 11 pills a day, does she need another?
Please let me know if anyone has experienced this as well.
Thank you.

Hi, I was on Prednisone for a little over a month for Crohn's disease. I had minor side effects while taking it: couldn't sleep, no patience, dehydrated, dry eyes. It is the side effects from AFTER stopping prednisone that concern me. I''ve been off Prednisone for 3 weeks and I think I am losing my hair and getting acne-that I didn't have before or during taking Prednisone. Anyone experience side effects that started after stopping the med?

I am really hoping someone can help me with the side effect issues I am having after taking Prednisone to cure a tumor on my larynx.. I was on the drug for six months.. taking 60 mg a day. It saved my life and at the same time it was just about to kill me, I am not kidding. The horrible effects it had on my body was really worse than the tumor that was taking my life. It would have almost been easy to die.
But today I'm very grateful for the miracle it did on my throat. I did not have a voice for many years.. today I can sing and that makes it's a great gift.
I was wondering, after being on it for so long and coming off nice and slowly, should my joints be in this much pain? My body aches are horrible.. all the muscles hurt and that never seems to go aways. Is this normal?

I have beenon lipitor for more than five years. I now have unbearable pains in my shoulders which are only relieved with antiinflammatories. I also have pains in my right foot which is sometimes very difficult to walk on. My Dr says ok go off lipitor but risk heart attack/stroke. I am getting to the point that the pain is so debilitating that Idon't care.

I have been reading the posts with great interest, and as a frequent prednisone flyer, I have a Canadian perspective that may or may not be helpful. (Please be patient as typing and prednisone don't mix with me :>)

But back to the point. During my years of prednisone useage, I have always been told that long term prednisone use shuts down the adrenal glands, not enhances it. Which is why after a period of two weeks,(the time it take for them to shut down approximately, continued use of prednisone takes over what the adrenal glands formally did. (ie. regulate metabolism, and provides resistance to stress; ie. temperature extremes, high altitudes, bleeding, infection, surgery, trauma, dental work and good old stress. It also has the bonus of raising blood pressure if and when a body needs it.) A lot of the side effects I have read come from the prednisone directly, and indirectly from non-functioning adrenal glands. Furthermore, we are told it takes roughly a year (sometimes longer), for full adrenal gland function to come back, and why, if during this time you do need surgery, dental work, or get an infection, or in an accident, it is not uncommon to have to go back on the prednisone until the 'stress' is fixed. The symptoms of low pressure (feeling faint, sweating, dizzy etc.) is usually the first sign that the adrenal glands are not working at full capacity yet.

Knowing all of that, I sincerely wish I had known that if one is depressed, anxious or suffering from panic attacks prednisone compounds the emotional problems greatly. Or
simply creates them as side effects. If you have existing psychological difficulties, sleeping 2 hours in 24, massive, unpredictable mood swings, (for me it was not so much mood
'swings' per se, more like bad, worse, and would someone please put me out of my misery.) For me, I know prednisone turns me into a 'speedfreak'. I can't sit still, can't talk, walk or smoke fast enough. I was very lucky after a stressful last year, and taking 50 mgs of predisone for 4 months, when I finally crashed, I spent 6 weeks in a psych ward basically to
contain me until I had been weaned off of the prednisone. (Ironically enough, it was a year ago tomorrow when I was hopitalized.)

So today I started taking 50 mgs of prednisone, and can already feel my heart and pulse rate excelerating. Fortunately, I no longer have the emotional distress, but during this summer I developed edema (45 pounds in a month), and high blood pressure. Both the doctor who prescribed it and the pharmacist who fill it assured me prednisone does not affect either. It only took about a minute and a half on the 'net to find out that wasn't true, (Everyone who already knew that feel free to giggle and roll your eyes a bit) after spending months working on getting the edema/HBP under 'reasonable' control. (At this point, I eat pizza and my eyes go blurry.) In closing I would be curious if any other readers have edema and/or high blood pressure before taking prednisone, and if/how much/in what way your experience has been in mixing the two.

Thank you.

I have been taking Lipitor for about 18 months. Recently, I started having a numbness in my lower buttocks and genitals. I went to see a Urologist iand he could not find anything wrong. I went to see a Cardiologist and he is going to order different tests. I started removing meds that I was taking and Lipitor is the last one I honestly perceive that this is the cause of my problems. I will know shortly if the feelings comes back and numbness leaves me. I also started taking CQ-10 and fish oils to lower my blood pressure and create cleaner arteries and etc. My BP is becoming normal and I am feeling better. I am afraid of Lipitor.

I started taking Levaquin on February 12,2005.My doctor gave my 500mg. for 10 days for a sinus infection. I had finished taking another antibiotic about 2 weeks before starting this one because I had another infection.The sinus infection got better but the muscle and joint aches have been horrible.I am 41 years old but feel like I am 90.It has been a week and a half since I finished it and I still feel lousy.I have been taking fish oils and magnessium but I know it takes a few weeks to work.Any suggestions from anyone on how long this will last or if there is anything to take to ease the discomfort?Thanks!

You know, I almost feel guilty at being the only success story to date here. Still taking 5mg. Zestril before bed every night. I insisted on this brand with my doctor as others were causing side effects. Having said that the British National Health Service contributes to supplies so it costs me just over £6 every order which can last up to two months. Interested to read opinions that Lisinopril is not necessarily for High BP. Now, if it's any help to you at all, can I suggest dietary changes too. I have for some weeks switched to Soya Milk and ceased (nearly) all dairy products (farmers practically stuff fat down your throats in the UK!). No chocolate either. Switch to a Soya based spread for putting on bread. Fish oils are also greatly beneficial, i.e. sardine, tuna, cod (cod liver oil) etc. I took my BP the other day (12 hours after the last tablet) and it still gave me the satisfactory reading of 122/75. The highest it seems to go now is about 140/85. Last year readings were around 150/98. I'm not so sure about taking lots of Coke (caffeine) to stay alert as someone suggested - doesn't this actually RAISE BP like smoking or alcohol? Good luck, stay well.